• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

Molecular temporal bone pathology: IV. Analysis of DNA template length using mitochondrial PCR primers.

作者信息

Wackym P A, Kerner M M, Grody W W

机构信息

Department of Otolaryngology and Communication Sciences, Medical College of Wisconsin, Milwaukee 53226, USA.

出版信息

Laryngoscope. 1998 Aug;108(8 Pt 2 Suppl 88):4-7. doi: 10.1097/00005537-199808001-00002.

DOI:10.1097/00005537-199808001-00002
PMID:9707260
Abstract

The focus of this study was to identify, via molecular biology techniques, the length of the DNA templates present in individual archival celloidin-embedded human temporal bone sections. Earlier studies have suggested that the maximum template length present in these tissues is on the order of 471 base pair (bp). Polymerase chain reaction (PCR) amplification of 92 bp, 121 bp, 471 bp, and 609 bp regions of mitochondrial DNA (mtDNA), extracted from single archival celloidin-embedded human temporal bone sections, was used to assess the length of the template DNA extracted. These data are crucial to determine the limits of applying PCR technology to amplify specific genomic DNA targets located within the human inner ear. The results described should be of value to those investigators extracting DNA from archival individual human temporal bone sections for polymerase chain reaction assays of specific genetic alterations or infectious agents associated with temporal bone pathologies.

摘要

相似文献

1
Molecular temporal bone pathology: IV. Analysis of DNA template length using mitochondrial PCR primers.
Laryngoscope. 1998 Aug;108(8 Pt 2 Suppl 88):4-7. doi: 10.1097/00005537-199808001-00002.
2
Characterization of DNA extracted from archival celloidin-embedded human temporal bone sections.
Am J Otol. 1995 Jan;16(1):14-20.
3
Polymerase chain reaction amplification of DNA from archival celloidin-embedded human temporal bone sections.从存档的火棉胶包埋的人类颞骨切片中进行DNA的聚合酶链反应扩增。
Laryngoscope. 1993 Jun;103(6):583-8. doi: 10.1288/00005537-199306000-00001.
4
Amplification of mitochondrial DNA from archival temporal bone specimens.从存档颞骨标本中扩增线粒体DNA。
Laryngoscope. 1995 Jan;105(1):28-34. doi: 10.1288/00005537-199501000-00009.
5
Amplification of RNA from archival human temporal bone sections.从存档的人类颞骨切片中扩增RNA。
Laryngoscope. 1999 Apr;109(4):617-20. doi: 10.1097/00005537-199904000-00018.
6
[Extraction, amplification, recombination and sequencing of the mitochondrial DNA from celloidin embedded human temporal bone sections].
Zhonghua Er Bi Yan Hou Ke Za Zhi. 1998 Aug;33(4):206-9.
7
Mitochondrial DNA deletions associated with aging and possibly presbycusis: a human archival temporal bone study.与衰老及可能的老年性聋相关的线粒体DNA缺失:一项人类颞骨存档研究
Am J Otol. 1997 Jul;18(4):449-53.
8
Detection of mitochondrial DNA from human inner ear using real-time polymerase chain reaction and laser microdissection.利用实时聚合酶链反应和激光显微切割技术检测人内耳中的线粒体DNA。
Acta Otolaryngol. 2005 Jul;125(7):697-701. doi: 10.1080/00016480510027510.
9
Technical report: laser microdissection of cochlear structures from celloidin embedded human temporal bone tissues and detection of the mitochondrial DNA common deletion using real time PCR.技术报告:从火棉胶包埋的人类颞骨组织中对耳蜗结构进行激光显微切割,并使用实时PCR检测线粒体DNA常见缺失。
Hear Res. 2008 Oct;244(1-2):1-6. doi: 10.1016/j.heares.2008.07.007. Epub 2008 Jul 31.
10
Association of mitochondrial DNA deletions and cochlear pathology: a molecular biologic tool.线粒体DNA缺失与耳蜗病理学的关联:一种分子生物学工具。
Laryngoscope. 1996 Jun;106(6):777-83. doi: 10.1097/00005537-199606000-00021.

引用本文的文献

1
Identification of a genetic variant underlying familial cases of recurrent benign paroxysmal positional vertigo.家族性复发性良性阵发性位置性眩晕病例的遗传变异鉴定。
PLoS One. 2021 May 6;16(5):e0251386. doi: 10.1371/journal.pone.0251386. eCollection 2021.